Search results for "bond"

showing 10 items of 3527 documents

Ion equilibrium in lichen surrounding.

2003

In laboratory conditions, the ionic equilibriums between a solution and a cation-active layer of epiphytic lichens Hypogymnia physodes immersed in the solution were examined. It was found that such equilibriums, due to exchange of mobile cations: H, Na, K, Ca, and Mg, are established in natural conditions between a lichen and atmospheric water.

Atmospheric waterIon TransportIon exchangeLichensChemistryBiophysicsIonic bondingGeneral MedicineHydrogen-Ion ConcentrationIonIon ExchangeEnvironmental chemistryCationsElectrochemistryEpiphytePhysical and Theoretical ChemistryLichenHypogymnia physodesBioelectrochemistry (Amsterdam, Netherlands)
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Compact two-electron wave function for bond dissociation and Van der Waals interactions: A natural amplitude assessment

2014

Electron correlations in molecules can be divided in short range dynamical correlations, long range Van der Waals type interactions and near degeneracy static correlations. In this work we analyze for a one-dimensional model of a two-electron system how these three types of correlations can be incorporated in a simple wave function of restricted functional form consisting of an orbital product multiplied by a single correlation function $f(r_{12})$ depending on the interelectronic distance $r_{12}$. Since the three types of correlations mentioned lead to different signatures in terms of the natural orbital (NO) amplitudes in two-electron systems we make an analysis of the wave function in t…

Atomic Physics (physics.atom-ph)General Physics and AstronomyFOS: Physical sciencesPhysics - Atomic Physicssymbols.namesakeCondensed Matter - Strongly Correlated ElectronsAtomic orbitalQuantum mechanicsPhysics - Chemical PhysicsPhysics::Atomic PhysicsSDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryWave functionAnsatzPhysicsChemical Physics (physics.chem-ph)Quantum Physics/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyta114Electronic correlationStrongly Correlated Electrons (cond-mat.str-el)Computational Physics (physics.comp-ph)Diatomic molecule3. Good healthBond lengthAmplitudesymbolsvan der Waals forceQuantum Physics (quant-ph)Physics - Computational Physics
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Ab initio study of the C60+Na system

2004

Abstract In this work we present the first CAS-CI calculation of the potential-electronic curves for the lowest states of the C 60 +Na system using a set of local orbitals. These orbitals permit to select a small active space describing the ionic interaction between the C 60 and the Na atom. A binding energy of about 3 eV has been found, a value substantially larger than previous theoretical results.

Atomic orbitalLinear combination of atomic orbitalsChemistryExcited stateBinding energyAb initioIonic bondingMolecular orbitalComplete active spacePhysical and Theoretical ChemistryAtomic physicsCondensed Matter PhysicsBiochemistryJournal of Molecular Structure: THEOCHEM
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Metal-support and preparation influence on the structural and electronic properties of gold catalysts

2006

Abstract Nanostructured gold catalysts supported on CeO2 and SiO2 were prepared by the deposition–precipitation (DP) and the solvated metal atom dispersion (SMAD) techniques. The structural and electronic properties of the catalysts were investigated by X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS) and X-ray photoelectron spectroscopy (XPS). Gold was found as small metal nanoparticles (cluster size ∼2 nm) in the SMAD-prepared samples and in ionic state in the DP catalysts. The catalytic activity of the samples was tested in the reaction of low temperature CO oxidation. Gold nanosized particles in a pure metallic state exhibited a worse catalytic performance, both on ceria and…

Au/SiO2Cerium oxideX-ray absorption spectroscopyAbsorption spectroscopyChemistryProcess Chemistry and TechnologyInorganic chemistryIonic bondingCO oxidationCatalysisXANESCatalysisParticle size effectMetalTransition metalX-ray photoelectron spectroscopyOxidation state of goldAu/CeO2visual_artvisual_art.visual_art_mediumXPS
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Simplified analytical model for moment–axial force domain in the presence of shear in R.C. members externally strengthened with steel cages

2015

Equations for a hand calculation of moment–axial force domain in the presence of shear for R.C. beam/column externally strengthened with steel angles and strips are developed. The analytical derivation is made assuming, for axial load and flexure, the equivalent stress-block parameters for internal forces, considering the confinement effects induced in the concrete core by external cages both in the cases of strips or angles yielding. Limit states due to bond failure, concrete crushing and yielding of steel angles and strips in flexure and in shear, including moment-to-shear interaction, are considered. The proposed model gives results in a good agreement with available experimental data an…

Axial force–moment interaction; Concrete beams; Concrete columns; Shear–moment interaction; Steel angles; Strengthening; Strips; Building and Construction; Civil and Structural Engineering; Mechanics of Materials; Materials Science (all)Materials scienceAxial force–moment interactionMaterials ScienceConcrete beams0211 other engineering and technologiesBond failureConcrete beam020101 civil engineering02 engineering and technologySTRIPSSteel angles0201 civil engineeringlaw.inventionlawStrips021105 building & constructionConcrete columnsMechanics of MaterialGeneral Materials ScienceCivil and Structural EngineeringHand calculationShear–moment interactionbusiness.industryBuilding and ConstructionStructural engineeringSettore ICAR/09 - Tecnica Delle CostruzioniShear (geology)Mechanics of MaterialsSteel angleSolid mechanicsStrengtheningAxial loadStripMaterials Science (all)Axial forcebusinessInternal forcesConcrete columnMaterials and Structures
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Synthesis of aryl azides: A probe reaction to study the synergetic action of ultrasounds and ionic liquids

2011

Abstract The combined effect of ultrasounds and ionic liquids was used to perform the synthesis of aryl azides by nucleophilic aromatic substitution in ionic liquid/[1-butyl-3-methylimidazolium][N 3 ] binary mixtures. The ultrasounds efficiency was analyzed as a function of the substrate and of the ionic liquid structure. In the first case, both 6π and 10π electrons aryl halides were considered. As far as the ionic liquid structure is concerned, both aromatic and aliphatic ionic liquids were taken into account. Among aromatic cations, the effects due to different ability in giving hydrogen bond or π–π interactions were considered. The use of a geminal ionic liquid having an aromatic spacer …

AzidesAcoustics and UltrasonicsInorganic chemistryIonic LiquidsHalideChemistry Techniques SyntheticPhotochemistryIonInorganic Chemistrychemistry.chemical_compoundNucleophilic aromatic substitutionChemical Engineering (miscellaneous)Environmental ChemistryUltrasonicsRadiology Nuclear Medicine and imagingMolecular StructureGeminalHydrogen bondArylOrganic ChemistrySubstrate (chemistry)StereoisomerismSettore CHIM/06 - Chimica OrganicachemistryIonic liquidIonic liquids Ultrasounds Aryl azides Nucleophilic aromatic substitutionUltrasonics Sonochemistry
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Direct subphthalocyanine conjugation to bombesin vs. indirect conjugation to its lipidic nanocarrier

2016

International audience; Bombesin (BBN) was covalently bound to graftable subphthalocyanine (SubPc) or to a cholesterol derivative, a component of a liposome that encapsulates non-graftable SubPc. The latter bioconjugation approach was suitable to address the stability of SubPc and was achieved by copper-free click-chemistry on the outer-face of the liposome. Liposomes were purified (FPLC) and then analyzed in size (outer diameter about 60 nm measured by DLS). In vitro binding studies allowed to determine the IC50 13.9 nM for one component of the liposome, cholesterol, conjugated to BBN. Hence, azido- (or alkynyl-) liposomes give fluorophores with no reactive functional group available on th…

AzidesIndolesStereochemistryefficacyConjugated systemIsoindoles010402 general chemistry01 natural sciencesBiochemistry[ CHIM ] Chemical Scienceschemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesPhysical and Theoretical Chemistrysilicon phthalocyaninesmelanoma-cellsLiposomeBioconjugationfluorescent[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryBombesinFast protein liquid chromatographyCombinatorial chemistryFluorescence0104 chemical sciencesNanostructuresmelanocyteschemistryphotodynamic therapyCovalent bondAlkynesLiposomesBombesinactivationNanocarriers
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4-hydroxy-ONN-azoxybenzene

2000

The oxidation of 4-hydroxy­azo­benzene provided a mixture of two azoxy compounds, which were separated by column chromatography. The isomer with the higher melting point appeared to belong to the α (ONN) series, as determined by X-ray diffraction. The mol­ecule, C12H10N2O2, is almost planar. The benzene rings are twisted by 11.7 (2) (substituted) and 4.1 (1)° (unsubstituted) with respect to the ONN plane. The mol­ecules are connected to one another by strong O—H⋯O hydrogen bonds forming chains extended along [001], which are bound by much weaker C—H⋯O hydrogen bonds forming layers in the bc plane.

AzoxyDiffractionPlane (geometry)Hydrogen bondStereochemistryGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographyColumn chromatographychemistryMelting pointBenzeneActa crystallographica. Section C, Crystal structure communications
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Disorder in the crystals of trans-4-fluoroazoxybenzene. Synthesis, spectral properties, crystal structures and DFT calculations

2005

Abstract Two crystals of trans-4-fluoroazoxybenzene were obtained using two different methods. Oxidation of 4-fluoroazobenzene provided crystals of trans-4-fluoroazoxybenzene (I) consisting of two isomers; 51% α (ONN) and 49% β (NNO) isomer. From trans-amino-azoxybenzenes in Schiemann reaction it were obtained crystals of trans-4-fluoro-NNO-azoxybenzenes (II, β isomer) containing 4.7% of the α-isomer according to the HPLC analysis. The crystal structures of I and II were determined by the X-ray diffraction method. In the crystal I two nitrogen atoms of azoxy bridge and fluorine atom are disordered. In the crystal II, there are two independent molecules of trans-4-fluoroazoxybenzene; the mol…

AzoxyTrans-4-fluoroazoxybenzeneHydrogen bondChemistryAromaticityCrystal structureOrganic ChemistryAromaticityCrystal structureDFT calculationsAnalytical ChemistryInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundMolecular geometryComputational chemistrySchiemann reactionMolecular symmetryDisorderMoleculeSpectroscopyJournal of Molecular Structure
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Orthorhombic polymorphs of twotrans-4-aminoazoxybenzenes

2002

The two isomeric compounds 4-amino-ONN-azoxybenzene [or 1-(4-aminophenyl)-2-phenyldiazene 2-oxide], i.e. the alpha isomer, and 4-amino-NNO-azoxybenzene [or 2-(4-aminophenyl)-1-phenyldiazene 2-oxide], i.e. the beta isomer, both C(12)H(11)N(3)O, crystallized from a polar solvent in orthorhombic space groups, and their crystal and molecular structures have been determined using X-ray diffraction. There are no significant differences in the bond lengths and valence angles in the two isomers, in comparison with their monoclinic polymorphs. However, the conformations of the molecules are different due to rotation along the Ar-N bonds. In the alpha isomer, the benzene rings are twisted by 31.5 (2)…

AzoxyValence (chemistry)X ray diffractionHydrogen bondStereochemistryCrystal structureChemical bondsGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyConformationsIsomersBond lengthCrystallographychemistry.chemical_compoundchemistryQuantum theoryMoleculeOrthorhombic crystal systemMolecular structureMonoclinic crystal systemActa Crystallographica Section C Crystal Structure Communications
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